Cure Talent are delighted to be partnered with a medical device manufacturer as they look to strengthen their Quality function. We have an exciting opportunity for a Quality System Engineer to join the team and take ownership of day-to-day quality processes within an established Quality Management System. As the new Quality System Engineer, you will be responsible for managing and maintaining core quality processes, supporting compliance with ISO 13485 and MDR requirements, and driving continuous improvement across the business. Reporting into the Quality Director, this is a hands-on role with broad exposure across audits, complaints, non-conformances, and GMP activities. Key Responsibilities * Manage and maintain the Quality Management System, ensuring ongoing compliance with applicable standards. * Oversee document control, including release, archiving, and maintenance of controlled documentation. * Manage non-conformances, supplier corrective actions, and root cause investigations. * Coordinate customer complaint investigations and generate technical reports as required. * Oversee internal, external, and supplier audits, ensuring actions are assigned and completed effectively. * Support deviation management and GMP review of manufacturing and quality records. * Provide training and quality induction to ensure company-wide understanding of quality procedures. * Support Management Review and Quality Imp...